A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671298



Internal ID9937403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:75168881..75175502hg38UCSC Ensembl
Outerchr18:75168724..75175655hg38UCSC Ensembl
Innerchr18:72880836..72887457hg19UCSC Ensembl
Outerchr18:72880679..72887610hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg386932
hg196932
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv605e199
Supporting Variantsessv5428985
SamplesNA19660
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671298
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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